Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree
Lynch syndrome (LS) is the most common hereditary colorectal cancer (CRCs) inherited in an autosomal-dominant manner. Here, we reported a multigeneration Chinese family clinically diagnosed with LS according to the Amsterdam II criteria. To identify the underlying causative gene for LS in this famil...
Main Authors: | , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2020-01-01
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Series: | Disease Markers |
Online Access: | http://dx.doi.org/10.1155/2020/8360841 |